Linked Data
MyVariant Identifiers:
chr21:g.45706574C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44286691C>T , CM000683.2:g.44286691C>T | GRCh38 |
| NC_000021.8:g.45706574C>T , CM000683.1:g.45706574C>T | GRCh37 |
| NC_000021.7:g.44531002C>T | NCBI36 |
| NG_009556.1:g.5812C>T , LRG_18:g.5812C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.267C>T MANE Select | ENSP00000291582.5:p.Arg89= | |
| ENST00000291582.5:c.267C>T | ENSP00000291582.5:p.Arg89= | |
| ENST00000527919.5:n.428C>T | ||
| ENST00000530812.5:n.436C>T | ||
| NM_000383.3:c.267C>T | NP_000374.1:p.Arg89= | |
| XM_011529551.1:c.267C>T | XP_011527853.1:p.Arg89= | |
| NM_000383.4:c.267C>T MANE Select | NP_000374.1:p.Arg89= |